A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112845



Internal ID20679885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150456901..150503600hg38UCSC Ensembl
chr4:151378053..151424752hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3846700
hg1946700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380250
Supporting Variants
Samples
Known GenesLRBA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00261


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